Canonical Allele Identifier: PA2827989615
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1511850
ClinVar RCV Id: RCV003773417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala2460Ser
CA16037645
NM_001354900.2:c.7378G>T